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Targeted gene knock-in by homology-directed genome editing using Cas9 ribonucleoprotein and AAV donor delivery

Realizing the full potential of genome editing requires the development of efficient and broadly applicable methods for delivering programmable nucleases and donor templates for homology-directed repair (HDR). The RNA-guided Cas9 endonuclease can be introduced into cells as a purified protein in com...

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Autores principales: Gaj, Thomas, Staahl, Brett T., Rodrigues, Gonçalo M. C., Limsirichai, Prajit, Ekman, Freja K., Doudna, Jennifer A., Schaffer, David V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5499784/
https://www.ncbi.nlm.nih.gov/pubmed/28334779
http://dx.doi.org/10.1093/nar/gkx154
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author Gaj, Thomas
Staahl, Brett T.
Rodrigues, Gonçalo M. C.
Limsirichai, Prajit
Ekman, Freja K.
Doudna, Jennifer A.
Schaffer, David V.
author_facet Gaj, Thomas
Staahl, Brett T.
Rodrigues, Gonçalo M. C.
Limsirichai, Prajit
Ekman, Freja K.
Doudna, Jennifer A.
Schaffer, David V.
author_sort Gaj, Thomas
collection PubMed
description Realizing the full potential of genome editing requires the development of efficient and broadly applicable methods for delivering programmable nucleases and donor templates for homology-directed repair (HDR). The RNA-guided Cas9 endonuclease can be introduced into cells as a purified protein in complex with a single guide RNA (sgRNA). Such ribonucleoproteins (RNPs) can facilitate the high-fidelity introduction of single-base substitutions via HDR following co-delivery with a single-stranded DNA oligonucleotide. However, combining RNPs with transgene-containing donor templates for targeted gene addition has proven challenging, which in turn has limited the capabilities of the RNP-mediated genome editing toolbox. Here, we demonstrate that combining RNP delivery with naturally recombinogenic adeno-associated virus (AAV) donor vectors enables site-specific gene insertion by homology-directed genome editing. Compared to conventional plasmid-based expression vectors and donor templates, we show that combining RNP and AAV donor delivery increases the efficiency of gene addition by up to 12-fold, enabling the creation of lineage reporters that can be used to track the conversion of striatal neurons from human fibroblasts in real time. These results thus illustrate the potential for unifying nuclease protein delivery with AAV donor vectors for homology-directed genome editing.
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spelling pubmed-54997842017-07-12 Targeted gene knock-in by homology-directed genome editing using Cas9 ribonucleoprotein and AAV donor delivery Gaj, Thomas Staahl, Brett T. Rodrigues, Gonçalo M. C. Limsirichai, Prajit Ekman, Freja K. Doudna, Jennifer A. Schaffer, David V. Nucleic Acids Res Methods Online Realizing the full potential of genome editing requires the development of efficient and broadly applicable methods for delivering programmable nucleases and donor templates for homology-directed repair (HDR). The RNA-guided Cas9 endonuclease can be introduced into cells as a purified protein in complex with a single guide RNA (sgRNA). Such ribonucleoproteins (RNPs) can facilitate the high-fidelity introduction of single-base substitutions via HDR following co-delivery with a single-stranded DNA oligonucleotide. However, combining RNPs with transgene-containing donor templates for targeted gene addition has proven challenging, which in turn has limited the capabilities of the RNP-mediated genome editing toolbox. Here, we demonstrate that combining RNP delivery with naturally recombinogenic adeno-associated virus (AAV) donor vectors enables site-specific gene insertion by homology-directed genome editing. Compared to conventional plasmid-based expression vectors and donor templates, we show that combining RNP and AAV donor delivery increases the efficiency of gene addition by up to 12-fold, enabling the creation of lineage reporters that can be used to track the conversion of striatal neurons from human fibroblasts in real time. These results thus illustrate the potential for unifying nuclease protein delivery with AAV donor vectors for homology-directed genome editing. Oxford University Press 2017-06-20 2017-03-02 /pmc/articles/PMC5499784/ /pubmed/28334779 http://dx.doi.org/10.1093/nar/gkx154 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Methods Online
Gaj, Thomas
Staahl, Brett T.
Rodrigues, Gonçalo M. C.
Limsirichai, Prajit
Ekman, Freja K.
Doudna, Jennifer A.
Schaffer, David V.
Targeted gene knock-in by homology-directed genome editing using Cas9 ribonucleoprotein and AAV donor delivery
title Targeted gene knock-in by homology-directed genome editing using Cas9 ribonucleoprotein and AAV donor delivery
title_full Targeted gene knock-in by homology-directed genome editing using Cas9 ribonucleoprotein and AAV donor delivery
title_fullStr Targeted gene knock-in by homology-directed genome editing using Cas9 ribonucleoprotein and AAV donor delivery
title_full_unstemmed Targeted gene knock-in by homology-directed genome editing using Cas9 ribonucleoprotein and AAV donor delivery
title_short Targeted gene knock-in by homology-directed genome editing using Cas9 ribonucleoprotein and AAV donor delivery
title_sort targeted gene knock-in by homology-directed genome editing using cas9 ribonucleoprotein and aav donor delivery
topic Methods Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5499784/
https://www.ncbi.nlm.nih.gov/pubmed/28334779
http://dx.doi.org/10.1093/nar/gkx154
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